Abstract: Described herein are methods of cleaning a tooth comprising administering a composition comprising a zinc amino acid halide complex to the oral cavity; and retaining the composition in the oral cavity for a time sufficient to form a precipitate.
Type:
Grant
Filed:
May 14, 2018
Date of Patent:
April 7, 2020
Assignee:
Colgate-Palmolive Company
Inventors:
Zhiqiang Liu, Long Pan, Shaotang Yuan, Jairajh Mattai, James Masters
Abstract: Synthetic methods for preparing deoxycholic acid and intermediates thereof, high purity synthetic deoxycholic acid, compositions and methods of use are provided. Also, provided are processes for the synthesis of 12-keto or 12-?-hydroxysteroids from ?-9,11-ene, 11-keto or 11-hydroxy-?-steroids. This invention is also directed to novel compounds prepared during the synthesis. This invention is also directed to the synthesis of deoxycholic acid starting from hydrocortisone.
Type:
Grant
Filed:
May 23, 2017
Date of Patent:
June 26, 2018
Assignee:
Kythera Biopharmaceuticals, Inc.
Inventors:
Robert M. Moriarty, Achampeta Rathan Prasad, John Gregory Reid, Roy A. Swaringen, Jr.
Abstract: The present invention relates to a new process of synthesis and to some new intermediates for the preparation of steroids with progestogen activity, more particularly, for the preparation of Desogestrel of formula (I). Said process is characterized by the regioselective reduction of the compound of formula (II) to give the intermediate of formula (III).
Abstract: The invention is directed to 11.beta.-aryl-17,17-spirothiolane substituted steroid compounds of formula (I) exhibiting binding to the progestin receptor. ##STR1## Also disclosed are methods of using and process of making the compounds.
Type:
Grant
Filed:
July 21, 1999
Date of Patent:
March 28, 2000
Assignee:
Research Triangle Institute
Inventors:
C. Edgar Cook, Rupa S. Shetty, John A. Kepler, David Y.-W. Lee
Abstract: The invention involves a two step chemical transformation of a steroidal 17-cyanohydrin (II) ##STR1## to a 17.alpha.-hydroxy-21-halo-20-keto steroid (IV) ##STR2## intermediate which can readily be converted to pharmaceutically useful corticoids.
Abstract: The present invention relates to 21-(3-carboxy-1-oxopropoxy) -17.alpha.-hydroxy-11.alpha.-(3,3-dimethyl-1-oxobutoxy)pregna-1,4-diene-3, 20 dione and pharmaceutically acceptable salts thereof which are useful steroid prodrugs.
Type:
Grant
Filed:
February 16, 1989
Date of Patent:
August 14, 1990
Assignee:
The Upjohn Company
Inventors:
John M. Braughler, Edward D. Hall, Wendell Wierenga, John M. McCall
Abstract: Novel 11.beta.-alkynylphenyl-19-nor-steroids of the formula ##STR1## wherein R.sub.1 is alkynyl of 2 to 8 carbon atoms optionally substituted with at least one member of the group consisting of --OH halogen, trialkylsilyl of 1 to 6 alkyl carbon atoms, alkoxy and alkylthio of 1 to 6 carbon atoms and dialkylamino of 1 to 6 alkyl carbon atoms having remarkably antiprogestomimetic and antiglucocorticoidal activity.
Type:
Grant
Filed:
April 30, 1987
Date of Patent:
March 27, 1990
Assignee:
Roussel Uclaf
Inventors:
Jean-Georges Teutsch, Michel Klich, Daniel Philibert